Absolute rate constants for hydrocarbon autoxidation. 24. Rate constants and Arrhenius parameters for reaction of tert-butylperoxy radicals with 3-methylpentane

1978 ◽  
Vol 56 (2) ◽  
pp. 170-175 ◽  
Author(s):  
J. A. Howard ◽  
J. H. B. Chenier ◽  
D. A. Holden

Autoxidation of 3-methylpentane in the presence of tert-butyl hydroperoxide gives, after reduction with triphenylphosphine, 3-methyl-3-pentanol and 3-methyl-2-pentanol as the major reaction products. The overall rate constant for reaction of (CH3)3COO· with this substrate at 30 °C is 0.008 ± 0.001 M−1 s−1 which consists of k/tertiary C—H = 0.007 ± 0.001 M−1 s−1 and k/secondary C—H = 0.0002 ± 0.0001 M−1 s−1. The products from cooxidation of cumene and 3-methylpentane in the presence of tert-butyl hydroperoxide are formed in yields which are consistent with these rate constants relative to a value of 0.16 M−1 s−1 for cumene. The Arrhenius equations for reaction of (CH3)3COO• with the t-C—H and s-C—H of 3-methylpentane relative to the Arrhenius equation for reaction of (CH3)3COO• with cumene (log (k10/M−1 s−1) = (8.7 ± 0.3) − (13.2 ± 0.4)/θ) are[Formula: see text]respectively, where θ = 2.303 RT kcal mol−1.

1980 ◽  
Vol 58 (24) ◽  
pp. 2808-2812 ◽  
Author(s):  
J. A. Howard ◽  
J. H. B. Chenier

Rate constants for abstraction of primary and secondary hydrogens from 2,2-dimethylbutane by the tert-butylperoxy radical at temperatures from 323 to 353 K have been determined from autoxidations and co-autoxidations in the presence of tert-butyl hydroperoxide. At 333 K the rate constant for abstraction of a secondary hydrogen is ~1.5 × 10−3 M−1 s−1 and the rate constants for abstraction of a primary hydrogen from the tert-butyl and methyl groups of 2,2-dimethylbutane are ~4 × 10−5 and ~6 × 10−5 M−5 s−1 respectively.


2020 ◽  
Vol 3 (2) ◽  
pp. 7-10
Author(s):  
Z. М. Коmarenska ◽  
◽  
М. V. Nykypanchuk ◽  
О. І. Маkota ◽  
L. P. Оliynyk ◽  
...  

A study of the process of activation of molybdenumboride catalyst in the reaction of epoxidation of octene-1 with tert-butyl hydroperoxide and the effect on this process of the initial concentration of octene-1, tert-butyl hydroperoxide and the amount of catalyst in the reaction mixture. As well as reaction products (tert-butyl alcohol and epoxy). It is shown that over time a new amorphous phase is formed on the surface of Mo2B, which actually catalyzes the epoxidation reaction of octene-1 with tert-butyl hydroperoxide. The formation of this phase is the reason for the acceleration of the rate of consumption of hydroperoxide and the selectivity of the formation of epoxide over time.


2012 ◽  
Vol 14 (13) ◽  
pp. 3384-3387 ◽  
Author(s):  
Erbo Shi ◽  
Ying Shao ◽  
Shulin Chen ◽  
Huayou Hu ◽  
Zhaojun Liu ◽  
...  

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